The von Recklinghausen neurofibromatosis region on chromosome 17--genetic and physical maps come into focus
- PMID: 2491773
- PMCID: PMC1715453
The von Recklinghausen neurofibromatosis region on chromosome 17--genetic and physical maps come into focus
Similar articles
-
The gene for von Recklinghausen neurofibromatosis (NF1) maps to the pericentromeric region of chromosome 17 in Chinese families.Genomics. 1991 Aug;10(4):1090-2. doi: 10.1016/0888-7543(91)90206-t. Genomics. 1991. PMID: 1916815
-
Flanking markers for the gene causing von Recklinghausen neurofibromatosis (NF1).Am J Hum Genet. 1989 Jan;44(1):30-2. Am J Hum Genet. 1989. PMID: 2491778 Free PMC article.
-
Linkage analysis in von Recklinghausen neurofibromatosis (NF1) with DNA markers for chromosome 17.Genomics. 1987 Dec;1(4):346-8. doi: 10.1016/0888-7543(87)90035-8. Genomics. 1987. PMID: 2896628
-
Progress towards identifying the neurofibromatosis (NF1) gene.Trends Genet. 1989 Jul;5(7):217-21. doi: 10.1016/0168-9525(89)90085-1. Trends Genet. 1989. PMID: 2506682 Review.
-
Molecular genetics of von Recklinghausen neurofibromatosis.Adv Hum Genet. 1991;20:267-307. doi: 10.1007/978-1-4684-5958-6_5. Adv Hum Genet. 1991. PMID: 1801591 Review. No abstract available.
Cited by
-
Chromosomes 17 and 22 involved in marker formation in neurofibrosarcoma in von Recklinghausen disease. A cytogenetic and in situ hybridization study.Hum Genet. 1990 Aug;85(3):337-42. doi: 10.1007/BF00206758. Hum Genet. 1990. PMID: 2118474
-
Genetics of cancer predisposition and progression.Clin Investig. 1993 Jun;71(6):488-502. doi: 10.1007/BF00180066. Clin Investig. 1993. PMID: 8353410 Review.
-
Loss of heterozygosity on chromosomes 17 and 18 in breast carcinoma: two additional regions identified.Proc Natl Acad Sci U S A. 1990 Oct;87(19):7737-41. doi: 10.1073/pnas.87.19.7737. Proc Natl Acad Sci U S A. 1990. PMID: 1977164 Free PMC article.
-
A genetic study of neurofibromatosis 1 in south-western Ontario. I. Population, familial segregation of phenotype, and molecular linkage.J Med Genet. 1991 Nov;28(11):746-51. doi: 10.1136/jmg.28.11.746. J Med Genet. 1991. PMID: 1685193 Free PMC article.
-
Genetic linkage and heterogeneity in type I Charcot-Marie-Tooth disease (hereditary motor and sensory neuropathy type I).Am J Hum Genet. 1990 Dec;47(6):915-25. Am J Hum Genet. 1990. PMID: 2239969 Free PMC article.
References
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Other Literature Sources
Research Materials